I believe that it will eventually be 16 internationally and federally legal, 280E-exempt, interstate, vertically-integrated, before-seed (genetic sequencing) to beyond-sold (patient post-use effectiveness followup questionaire data-mining), distribution system. I base this on a number of conversations with Section Chiefs in the Diversion Division. There are at least half a dozen companies in active pursuit of establishing such a system. Reply
“While past illegal conduct involving controlled substances does not automatically disqualify an applicant, it may weigh heavily against granting the registration,” I would suggest taking them at their word. If they say flatly that it won’t be a disqualification, it’s not one. On the other hand, if they say that it flat out is, they run into exactly the Catch-22 pointed out in the article. It seems extremely doubtful that they will disqualify you if you have crossed every eye and dotted every t along the way in becoming a state-licensed MEDICAL facility. If your state has a research license in its offerings, so much the better. Have your security already up to what FDA/DEA require of Controlled Substance manufacturers. It may be necessary to move to an Industrial Park model to have this be affordable for smaller enterprises. Speaking of which, there is room in this model for smaller growers/artisan growers if they are prepared to organize. Now the pitch. I do consulting. Reply
Hmmm.. would like to followup on this and find out more about what the DEA is currently doing. Anybody inside the DEA willing to comment? Reply